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CDMO Europe 2025
#CDMOEurope2025
Driving Innovation & Excellence in Outsourced Manufacturing
A New Era for Europe's CDMO Leaders Begins this November | Where Strategy Meets Precision and Nothing is Left to Chance
Munich
19
-
20
November 2025
00
Days
00
Hours
00
Mins
00
Secs
+
Attendees
300
Maximum Attendees
100
+
Companies
30
+
Speakers
20
+
Networking Hours
+
Case Studies
Interactive Sessions
About the Event
Where Strategy Meets Precision. And Nothing is Left to Chance
In an industry defined by complexity and speed, the smartest players know that not every stage demands more noise but rather sharper focus.
#CDMOEurope2025 isn’t a crowded expo floor or a passive lecture circuit; it’s a crafted, closed-door experience where no more than 300 hand-picked specialists will gather to exchange insights, accelerate partnerships, and shape the future of biologics manufacturing. This is where real conversations happen.
What Makes this Summit Different?
- Exclusivity by Design
This isn’t about how many people we can fit in a room - . Every delegate, every speaker, and every partner is carefully selected for strategic alignment. If you're here, it's because you matter. - Depth Over Buzzwords
Forget surface-level panels and recycled content. Expect off-the-record discussions, battle-tested case studies, and forward-thinking insights in an environment built for candour and clarity. - Precision Networking
From personalised meetings to executive roundtables, every interaction is intentional. You won’t need to sort through business cards - you’ll meet the right people, at the right time, with the right context.
Designed for the Visionaries of Contract Manufacturing
Focused on the critical inflection points facing CDMOs and biopharma innovators across Europe, you’ll engage in high-level dialogue on:
- Building agile, tech-enabled, future-proof manufacturing models
- Navigating cross-border partnerships and evolving EU regulatory frameworks
- Resilience, scalability, and sustainability in biologics outsourcing
- Managing talent and capacity in a competitive, post-pandemic ecosystem
Who Will You Meet?
Leaders from across the European biomanufacturing ecosystem — including:
- Heads of External Manufacturing & Strategic Partnerships
- CTOs, MSAT Directors, and Supply Chain Experts
- Founders and C-Level Executives from high-growth CDMOs
- Global Biopharma Decision-Makers with outsourcing mandates
Featuring real-time perspectives from organisations including Johnson & Johnson, Bayer, Sanofi, Abcellera, Amgen, and many more.
Attendance is Limited; Influence is Not
If you’re looking for a typical conference, this isn’t it. But if you’re looking to spend 2 days immersed in signal (not noise) with peers who match your ambition, #CDMOEurope2025 belongs on your calendar.
Agenda at a Glance
View the Key Themes for
CDMO Europe 2025
Day 1 | CDMO Strategy & Compliance
- Evaluating CDMO Capabilities
- Tech Transfer Simplified
- Regulatory Updates & Compliance
Day 2 | Advanced Manufacturing Technologies
- Cost Optimisation in Outsourcing
- Single-Use Technologies
- Aseptic Fill-Finish Excellence
- Supply Chain Resilience
Ready to attend?
Register today to secure your ticket.
Speakers
Esteemed Voices From the Industry
Our selected experts will share insights on the latest trends, challenges, and developments in this dynamic field. Engage in unique discussions, learn about cutting-edge scientific discoveries, and explore the future of biopharmaceuticals with these influential thought leaders.
Giulio Cavalli
Johnson & Johnson Innovative Medicine
Principal Lead, External Manufacturing
Giulio Cavalli
Principal Lead, External Manufacturing
Johnson & Johnson Innovative Medicine
Switzerland
Tamika Drummond
Abcellera
External MSAT Manager
Tamika Drummond
External MSAT Manager
Abcellera
Canada
Olusegun Adetunji
Sanofi
Global External Manufacturing & Supplier Stream Lead
Olusegun Adetunji
Global External Manufacturing & Supplier Stream Lead
Sanofi
Spain
Dr Ulrich Rümenapp
Bayer
Head of Launch Preparation & Co-ordination
Dr Ulrich Rümenapp
Head of Launch Preparation & Co-ordination
Bayer
Germany
Christian Simon
Sanofi
Head of Technical Transfer External Manufacturing
Christian Simon
Head of Technical Transfer External Manufacturing
Sanofi
Germany
Roman Mijnhart
Ultragenyx
Executive Director, Head of Quality EU
Roman Mijnhart
Executive Director, Head of Quality EU
Ultragenyx
Netherlands
Andreas Schaaf
Eleva Biologics
Managing Director/CSO
Andreas Schaaf
Managing Director/CSO
Eleva Biologics
Germany
Jenny Prange
MUVON Therapeutics AG
CTO and Co-Founder, Head of GMP Production
Jenny Prange
CTO and Co-Founder, Head of GMP Production
MUVON Therapeutics AG
Switzerland
Sonja Nicoll
Amgen
Senior Director - Biologics
Sonja Nicoll
Senior Director - Biologics
Amgen
Germany
Ralf Huss
Biom Biotech Cluster
Managing Director
Ralf Huss
Managing Director
Biom Biotech Cluster
Germany
Dr Pavan Beleyur Narayanaswamy
AATec Medical
Head of CMC and Regulatory Affairs
Dr Pavan Beleyur Narayanaswamy
Head of CMC and Regulatory Affairs
AATec Medical
Germany
Christopher Pawlak
Bayer
External Manufacturing Lead
Christopher Pawlak, Ph.D., had almost 2 decades in leadership position managing External Manufacturing and CDMOs in Pharmaceutical markets all over the globe. He oversaw global supplier management, external manufacturing operations, and strategic partnerships across the company’s biopharmaceutical network, manage finance of external manufacturing network. With over two decades of experience in pharmaceutical supply chain and procurement, he has led initiatives to enhance supplier performance, drive operational efficiency, and foster intercultural collaboration in global manufacturing.
In addition to his industry leadership, Dr. Pawlak serves as a lecturer and Executive Council member at the St. Gallen Integrated IMT Business School, reflecting his ongoing commitment to education and executive development. He is widely recognized as a thought leader in strategic supplier management, intercultural collaboration, and biomanufacturing innovation.
Christopher Pawlak
External Manufacturing Lead
Bayer
Switzerland
Chris Baldwin
Resolution Therapeutics
Vice President, Manufacturing and Supply
Chris Baldwin
Vice President, Manufacturing and Supply
Resolution Therapeutics
United Kingdom
Registration
Choose a plan that fits your role, company, and industry.
BIG PHARMA
£2050 + VAT
Early Bird
VAT exemptions will be applied where applicable in accordance with relevant regulations.
BIOPHARMA & ACADEMIC
£850 + VAT
Early Bird
VAT exemptions will be applied where applicable in accordance with relevant regulations.
For Companies Outside Singapore
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£2895 + VAT
Attendance Only
Partnership benefits not included
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Pre Conference Workshops & Other Sessions
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Frequently Asked Questions
How can I stay updated on event details and announcements?
To stay informed about event updates, including date, venue, and agenda, please subscribe to our newsletter on our event website. You can also follow our official social media channels for real-time updates and announcements.
What can I expect to learn and explore during the event?
The conference will provide a comprehensive learning experience covering various aspects of the dynamic biopharmaceutical industry, ensuring attendees gain valuable insights and knowledge.
What safety measures will be in place to ensure the safety of attendees?
We are committed to ensuring the safety and well-being of all attendees. We will implement rigorous safety measures in line with local health guidelines and regulations. Specific safety measures will be communicated closer to the event date to ensure they align with the most up-to-date health recommendations. Rest assured, your safety is our priority.
Is there a cancellation or refund policy if I can't attend after registering?
Yes, we have a cancellation and refund policy in place. Please refer to our “Cancellation Policy” on our website for details on how to request a refund if you are unable to attend.
Can I submit a presentation to be a speaker at this event?
We welcome presentation submissions. If you’re interested in speaking at the event, please visit this page on our website for submission guidelines and deadlines.
What type of professionals benefit most from attending?
Our event is designed to cater to a wide range of professionals within the biopharmaceutical industry, including researchers, scientists, executives, regulatory experts, and professionals involved in drug development and manufacturing.
What advantages does this conference offer participants?
Participants can expect to gain insights from industry experts, network with peers, and stay up-to-date with the latest trends and innovations in biopharmaceuticals
Are there networking opportunities or special events planned?
Yes, we have networking sessions, workshops, and social events scheduled throughout the event to facilitate connections and collaborations among attendees.
Are there sponsorship opportunities for this event?
Yes, we offer sponsorship and exhibition opportunities for businesses and organizations. Please visit our this page on our website for more information.
How can I register for the event?
To register for the event, you'll find multiple "register" buttons on this page to get started. You’ll find detailed instructions and options for registration, including pricing and deadlines.
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